TitleDoes vitamin E decrease heart attack risk? summary and implications with respect to dietary recommendations.
Publication TypeJournal Article
Year of Publication2001
AuthorsTraber MG
JournalJ Nutr
Volume131
Issue2
Pagination395S-7S
Date Published2001 Feb
ISSN0022-3166
KeywordsAnimals, Antioxidants, Heart Diseases, Humans, Models, Animal, Nutrition Policy, Risk Factors, Vitamin E
Abstract

The hypothesis that oxidative stress has a role in atherosclerosis rests on a large body of experimental work carried out in animal models of heart disease. The situation is more complex in humans, in that the results from vitamin E supplementation trials have been conflicting. Nonetheless, there is emerging information that alpha-tocopherol may play a critical role in maintaining the function of key cellular components in the atherosclerotic process through its ability to inhibit the activity of protein kinase C, a key player in many signal transduction pathways. alpha-Tocopherol modulates pathways of platelet aggregation, endothelial cell nitric oxide production, monocyte/macrophage superoxide production and smooth muscle cell proliferation. Regulation of adhesion molecule expression and inflammatory cell cytokine production by alpha-tocopherol has also been reported. More studies are required to relate alpha-tocopherol intakes to optimal tissue responses in humans.

DOI10.1093/jn/131.2.395S
Alternate JournalJ. Nutr.
PubMed ID11160568